5-METHYL-4-(2-THIAZOLYLAZO)RESORCINOL

Base Information

• Chemical Name: 5-METHYL-4-(2-THIAZOLYLAZO)RESORCINOL
• CAS No.: 37422-56-3
• Molecular Formula: C10H9N3O2S
• Molecular Weight: 235.266
• Hs Code.: 2934100090
• Mol file: 37422-56-3.mol

Synonyms:TAO~4-(2-Thiazolylazo)orcinol;5-methyl-4-thiazol-2-ylazo-benzene-1,3-diol;6-(2-THIAZOLYLAZO)ORCINOL;5-methyl-4-(2-thiazolylazo)-1,3-benzenediol;6-(2'-Thiazolylazo)orcin;5-Methyl-4-(2-thiazolylazo)-1,3-benzenediol,TAO;

Chemical Property of 5-METHYL-4-(2-THIAZOLYLAZO)RESORCINOL

Chemical Property:

• Melting Point: 211-213oC (dec.)(lit.)
• PSA: 106.31000
• LogP: 3.27810

Purity/Quality:

99% ^*data from raw suppliers

5-Methyl-4-(2-thiazolylazo)resorcinol 95% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Use Description: 5-Methyl-4-(2-thiazolyazo)resorcinol is a chemical compound with diverse applications across different fields. In the field of analytical chemistry, it is used as a reagent and colorimetric indicator for the detection and quantification of various metal ions, including copper and cobalt, in complex mixtures and solutions. Its role is crucial in analytical techniques like spectrophotometry, where it forms colored complexes with metal ions, allowing for precise measurements. Additionally, in the textile and dyeing industry, 5-METHYL-4-(2-THIAZOLYLAZO)RESORCINOL can find use as a dye and pigment, contributing to the vibrant coloration of fabrics and materials. Its adaptability as an analytical reagent and a colorant underscores its significance in advancing analytical chemistry and textile dyeing in various fields.

Technology Process of 5-METHYL-4-(2-THIAZOLYLAZO)RESORCINOL

There total 1 articles about 5-METHYL-4-(2-THIAZOLYLAZO)RESORCINOL which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

2-thiazolylamine (96-50-4) + orcinol (504-15-4) → 5-methyl-4-(2-thiazolylazo)resorcinol (37422-56-3)

Guidance literature:

Multistep reaction; (i) aq. NaNO₂, HCl, (ii) /BRN= 1071903/, (iii) aq. NaOAc;

Reference yield: 88.0%

2-chloroetyl vinyl ether (110-75-8) + 5-methyl-4-(2-thiazolylazo)resorcinol (37422-56-3) → 5-methyl-4-(2-thiazolylazo)resorcinoxy ethyl vinyl ether (1219448-30-2)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 80 ℃; for 15h;

DOI:10.1002/pola.23875

Reference yield:

ammonium metavanadate + 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyl-3H-tetrazol-2-ium chloride (146-68-9) + 5-methyl-4-(2-thiazolylazo)resorcinol (37422-56-3) → 2O2V(1+)*2C10H7N3O2S(2-)*2C19H13IN5O2(1+)

Guidance literature:

In chloroform; water;

DOI:10.5562/cca2436

upstream raw materials:

2-thiazolylamine

orcinol

Downstream raw materials:

5-methyl-4-(2-thiazolylazo)resorcinoxy ethyl vinyl ether

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